Perform

Product NDC
59316-108
11-digit product format
593160108
Labeler code
59316
Product ID
59316-108_2bd580d6-39b1-4892-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
GEL
Route
TOPICAL
Labeler
Performance Health LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2009-12-30
Marketing end
2019-12-31
Substance
MENTHOL
Active strength
31 mg/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59316-108-15ML - Milliliter59316-108d3fbe7a9-3e18-4f88-ae1d-c593b65ab9b112015-07-20